TY - JOUR
T1 - The evolution of antipsychotic switch and polypharmacy in natural practice - A longitudinal perspective
AU - Tsutsumi, Chisa
AU - Uchida, Hiroyuki
AU - Suzuki, Takefumi
AU - Watanabe, Koichiro
AU - Takeuchi, Hiroyoshi
AU - Nakajima, Shinichiro
AU - Kimura, Yoshie
AU - Tsutsumi, Yuichiro
AU - Ishii, Koichi
AU - Imasaka, Yasushi
AU - Kapur, Shitij
N1 - Funding Information:
Dr. Uchida has received grants, speaker's honoraria, or manuscript fees from Pfizer Health Research Foundation, GlaxoSmithKline, Otsuka Pharmaceutical, Dainippon Sumitomo Pharma, Janssen Pharmaceutical, and Pfizer within the past 5 years. Dr. Suzuki has received manuscript fees from Dainippon Sumitomo Pharma and Kyowa Hakko Kirin within the past 5 years. Dr. Takeuchi has received speaker's honoraria or manuscript fees from Dainippon Sumitomo Pharma, Eli Lilly, GlaxoSmithKline, Janssen Pharmaceutical, and Otsuka Pharmaceutical within the past 5 years. Dr. Nakajima has received grants from Pfizer and speaker's honoraria or manuscript fees from Dainippon Sumitomo Pharma, GlaxoSmithKline, Jannsen Pharmaceutical and Pfizer within the past 5 years. Dr. Imasaka has received speaker's honoraria from Eli Lilly, Pfizer, Meiji, GlaxoSmithKline, Janssen Pharmaceutical, and Otsuka within the past 5 years. Dr. Tsutsumi has received consultant fees or speaker's honoraria from Astellas Pharma, Eli Lilly, Otsuka Pharmaceutical, Dainippon Sumitomo Pharma, Janssen Pharmaceutical, GlaxoSmithKline, and Schering-Plough within the past 5 years. Dr. Watanabe has received grants, or consultant fees from Dainippon Sumitomo Pharma, Eli Lilly, GlaxoSmithKline, Janssen Pharmaceutical, and Pfizer, and received speaker's honoraria from Astellas Pharma, Dainippon Sumitomo Pharma, Eli Lilly, GlaxoSmithKline, Janssen Pharmaceutical, Meiji, Otsuka Pharmaceutical, Pfizer, and Yoshitomiyakuhin within the past 5 years. Dr. Kapur has received grant support from AstraZeneca and GSK; and has served as consultant and/or speaker for AstraZeneca, Bioline, BMS-Otsuka, Eli Lilly, Janssen (J&J), Lundbeck, NeuroSearch, Pfizer, Roche, Servier and Solvay Wyeth. Other authors have nothing to disclose.
Funding Information:
This work was funded by Japan Research Foundation for Clinical Pharmacology, Tokyo, Japan (HU), Research Group for Schizophrenia, Tokyo, Japan (HU), Grant-in-Aid for Young Scientists-B from the Ministry of Education, Culture, Sports, Science and Technology, Tokyo, Japan (HU), Japanese Society of Clinical Neuropsychopharmacology, Tokyo, Japan (TS), Government of Canada Post-Doctoral Research Fellowships, Ottawa, Canada (TS), Kanae Foundation, Tokyo, Japan (TS) and Mochida Memorial Foundation, Tokyo, Japan (TS).
PY - 2011/8
Y1 - 2011/8
N2 - Objective: Most patients with schizophrenia first start with a single antipsychotic, and yet most finally end up 'switching' or using 'polypharmacy'. The objective of this study was to examine the evolution of antipsychotic switch and polypharmacy in the real-world from a longitudinal perspective. Methods: A systematic review of longitudinal antipsychotic prescriptions in 300 patients with schizophrenia (ICD-10) for up to 2. years after their first visit to one of the 4 participating psychiatric clinics in Tokyo, Japan between January, 2007 and June, 2008, was conducted. Reasons for prescription change were also examined. The evolution of switching and polypharmacy was studied, and prescribed doses were compared to suggested dose ranges by the Texas Medication Algorithm Project (TMAP). Results: 208 patients started their antipsychotic treatment with monotherapy. 34.1% of the patients gave up monotherapy with an initial antipsychotic to move to antipsychotic switch (27.4%) and/or polypharmacy (17.8%) within 2. years. The main reason for antipsychotic switch was 'ineffectiveness'; interestingly, this happened despite the fact that the monotherapy dose was below the recommended range in 47.4% of the antipsychotic switch. In a subgroup of 100 patients who started as antipsychotic-free, 2-year prevalence rates of switching and antipsychotic polypharmacy were 27.0% and 18.0%, respectively, and polypharmacy was resorted to after a median of 1 antipsychotic had been tried for 84. days (median). Conclusions: These findings raise a concern that physicians may perform an antipsychotic switch without exploring the entire dose range and resort to antipsychotic polypharmacy without trying an adequate number of antipsychotics.
AB - Objective: Most patients with schizophrenia first start with a single antipsychotic, and yet most finally end up 'switching' or using 'polypharmacy'. The objective of this study was to examine the evolution of antipsychotic switch and polypharmacy in the real-world from a longitudinal perspective. Methods: A systematic review of longitudinal antipsychotic prescriptions in 300 patients with schizophrenia (ICD-10) for up to 2. years after their first visit to one of the 4 participating psychiatric clinics in Tokyo, Japan between January, 2007 and June, 2008, was conducted. Reasons for prescription change were also examined. The evolution of switching and polypharmacy was studied, and prescribed doses were compared to suggested dose ranges by the Texas Medication Algorithm Project (TMAP). Results: 208 patients started their antipsychotic treatment with monotherapy. 34.1% of the patients gave up monotherapy with an initial antipsychotic to move to antipsychotic switch (27.4%) and/or polypharmacy (17.8%) within 2. years. The main reason for antipsychotic switch was 'ineffectiveness'; interestingly, this happened despite the fact that the monotherapy dose was below the recommended range in 47.4% of the antipsychotic switch. In a subgroup of 100 patients who started as antipsychotic-free, 2-year prevalence rates of switching and antipsychotic polypharmacy were 27.0% and 18.0%, respectively, and polypharmacy was resorted to after a median of 1 antipsychotic had been tried for 84. days (median). Conclusions: These findings raise a concern that physicians may perform an antipsychotic switch without exploring the entire dose range and resort to antipsychotic polypharmacy without trying an adequate number of antipsychotics.
KW - Antipsychotic
KW - Dose
KW - Polypharmacy
KW - Prescription
KW - Schizophrenia
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U2 - 10.1016/j.schres.2011.05.013
DO - 10.1016/j.schres.2011.05.013
M3 - Article
C2 - 21624824
AN - SCOPUS:79960335818
VL - 130
SP - 40
EP - 46
JO - Schizophrenia Research
JF - Schizophrenia Research
SN - 0920-9964
IS - 1-3
ER -